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rs151341145

From SNPedia

Merged intors1050556
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341145(G;T)
Make rs151341145(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356809
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341145
ebirs151341145
HLIrs151341145
Exacrs151341145
Varsomers151341145
Maprs151341145
PheGenIrs151341145
hapmaprs151341145
1000 genomesrs151341145
hgdprs151341145
ensemblrs151341145
gopubmedrs151341145
geneviewrs151341145
scholarrs151341145
googlers151341145
pharmgkbrs151341145
gwascentralrs151341145
openSNPrs151341145
23andMers151341145
23andMe allrs151341145
SNP Nexus

SNPshotrs151341145
SNPdbers151341145
MSV3drs151341145
GWAS Ctlgrs151341145
StatusMerged into rs1050556
Max Magnitude0
ClinVar
Risk rs151341145(T;T)
Alt rs151341145(T;T)
Reference rs151341145(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324586C>A
CLNSRC
CLNACC